Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g35140 | A03 | 16257914 | G | A | downstream_gene_variant | MODIFIER | c.*3905C>T| |
S63 |
2 | BAA03g35140 | A03 | 16257944 | C | T | downstream_gene_variant | MODIFIER | c.*3875G>A| |
S210 S225 |
3 | BAA03g35140 | A03 | 16258557 | C | T | downstream_gene_variant | MODIFIER | c.*3262G>A| |
S16 |
4 | BAA03g35140 | A03 | 16259347 | C | T | downstream_gene_variant | MODIFIER | c.*2472G>A| |
S23 |
5 | BAA03g35140 | A03 | 16259490 | C | T | downstream_gene_variant | MODIFIER | c.*2329G>A| |
S174 |
6 | BAA03g35140 | A03 | 16259735 | G | A | downstream_gene_variant | MODIFIER | c.*2084C>T| |
S276 |
7 | BAA03g35140 | A03 | 16260461 | C | T | downstream_gene_variant | MODIFIER | c.*1358G>A| |
S79 S91 |
8 | BAA03g35140 | A03 | 16262422 | G | A | intron_variant | MODIFIER | c.1530-543C>T| |
S256 |
9 | BAA03g35140 | A03 | 16264280 | C | T | missense_variant | MODERATE | c.1318G>A|p.Ala440Thr |
S294 |
10 | BAA03g35140 | A03 | 16264544 | G | A | intron_variant | MODIFIER | c.1195-47C>T| |
S90 |
11 | BAA03g35140 | A03 | 16265503 | G | A | missense_variant | MODERATE | c.811C>T|p.Leu271Phe |
S88 |
12 | BAA03g35140 | A03 | 16265892 | C | T | missense_variant | MODERATE | c.595G>A|p.Val199Met |
S281 |
13 | BAA03g35140 | A03 | 16266008 | C | T | missense_variant | MODERATE | c.479G>A|p.Ser160Asn |
S62 |
14 | BAA03g35140 | A03 | 16266894 | G | A | upstream_gene_variant | MODIFIER | c.-82C>T| |
S59 |
15 | BAA03g35140 | A03 | 16267040 | C | T | upstream_gene_variant | MODIFIER | c.-228G>A| |
S153 |
16 | BAA03g35140 | A03 | 16269773 | C | T | upstream_gene_variant | MODIFIER | c.-2961G>A| |
S105 S106 |